Figure 3
Figure 3. Distribution and quantification of FGFR1/2+ mesenchymal cells after sublethal TBI. (A) Ten days after irradiation (10 DPI) at 9 Gy, the periosteum showed evidence of intense remodeling and FGFR2+ cells were observed in vascularized PN+ canals on the cortical bone surface (see also supplemental Figure 1B). Scale bar indicates 50 μm. (B) Flow cytometric quantification of FGFR1+ and FGFR2+ mesenchymal cells in whole bones 10 days after sublethal irradiation. (C) Cells in the R2 region (Lin−/CD45−/FGFR1 or 2+) were compared with total cell numbers obtained from 5 nonirradiated control mice and 10 irradiated test mice. The frequency (%) of FGFR1/2+ cells was increased after irradiation, but their absolute number was relatively stable, suggesting that these cells are radio-resistant. APC indicates allophycocyanin.

Distribution and quantification of FGFR1/2+ mesenchymal cells after sublethal TBI. (A) Ten days after irradiation (10 DPI) at 9 Gy, the periosteum showed evidence of intense remodeling and FGFR2+ cells were observed in vascularized PN+ canals on the cortical bone surface (see also supplemental Figure 1B). Scale bar indicates 50 μm. (B) Flow cytometric quantification of FGFR1+ and FGFR2+ mesenchymal cells in whole bones 10 days after sublethal irradiation. (C) Cells in the R2 region (Lin/CD45/FGFR1 or 2+) were compared with total cell numbers obtained from 5 nonirradiated control mice and 10 irradiated test mice. The frequency (%) of FGFR1/2+ cells was increased after irradiation, but their absolute number was relatively stable, suggesting that these cells are radio-resistant. APC indicates allophycocyanin.

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